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Core-Mark Mid-Continent, Inc. — FDA Facility Profile

FEI 1211924

Core-Mark Mid-Continent, Inc. is an FDA-inspected facility (FEI 1211924) located in Gardiner, ME, US. RegDataLab tracks 4 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Nov 4, 2020: No Action Indicated (NAI)
Inspections on record
4 (1 VAI, 3 NAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Nov 4, 2020No Action Indicated (NAI)No citations listed
Sep 7, 2016No Action Indicated (NAI)No citations listed
Feb 4, 2015Voluntary Action Indicated (VAI)No citations listed
Jul 16, 2012No Action Indicated (NAI)No citations listed

Facility details

Company
Core-Mark Mid-Continent, Inc.
Location
Gardiner, ME (US)
Source
inspections

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.